Hydrochloric Acid → HCID 20511278, compound

HRID 1164537Notes

Reaction equation

HRID 1164537 reaction equation
[ClH:1].[OH:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][C:11]=1[OH:12])[CH2:6][CH2:7][NH2:8].C(O[CH:16](OCC)[CH2:17][O:18][C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1)C.Cl>C(O)CCC>[ClH:1].[ClH:1].[N:22]1[CH:23]=[CH:24][C:19]([O:18][CH2:17][CH:16]2[C:9]3[C:5](=[CH:4][C:3]([OH:2])=[C:11]([OH:12])[CH:10]=3)[CH2:6][CH2:7][NH:8]2)=[CH:20][CH:21]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 65340Dopamine HydrochlorideHCID 20511268HCID 20511268, compound

Product 1

HCID 20511278HCID 20511278, compoundYield 215.2%

Reagents, catalysts & solvents 1

HCID 2631-ButanolSolvent2×

Procedure

A mixture of 3,4-dihydroxyphenethylamine hydrochloride (2.4 g), (4-pyridyl)oxyacetaldehyde diethyl acetal (3.7 g), n-butanol (40 ml) and 1 N-hydrochloric acid (20 ml) was refluxed for 15 hours under stirring. After the reaction, n-butanol was distilled off from the reaction mixture under reduced pressure. The residue was dissolved in water, and the solution was washed twice with chloroform and once with ether. The aqueous layer was concentrated, and the oily residue was allowed to stand to give crystals of 1-(4-pyridyl)oxymethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline dihydrochloride (4.7 g). The product was recrystallized from aqueous methanol to give needles, mp 250° to 255° C. (dec.).

Workup

  1. temperaturewas refluxed for 15 hours
  2. distillationwas distilled off from the reaction mixture under reduced pressure
  3. dissolutionThe residue was dissolved in water
  4. washthe solution was washed twice with chloroform and once with ether
  5. concentrationThe aqueous layer was concentrated

Sources & evidence

ORD record
ord-0d9e3001d89c455e8e41ddc1c4ef5272
Source dataset
uspto-grants-1983_01
Patent number
US04370332

Reaction notes

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